Empleos de Regulatory Submissions

The Precision Medicine Director leads precision medicine strategies for clinical programs, focusing on biomarker and diagnostic activities to enable patient selection and biomarker-based clinical…

The Precision Medicine Director leads the development and execution of precision medicine strategies for clinical programs, focusing on biomarker and companion diagnostic activities to enable patient…

IQVIA Spain is hiring a junior Clinical Research Associate to join a sponsor-dedicated team, performing site selection, initiation, monitoring, and close-out visits while ensuring compliance with…

The Regulatory Affairs Administrator at Puig is responsible for gathering and analyzing technical documentation for cosmetic finished products, preparing submission dossiers for international…

This Director, Medical Safety role at IQVIA in Madrid involves leading medical review of clinical trial and post-marketing safety data, providing medical oversight, and supporting safety governance.

AstraZeneca is hiring a Director, Principal Patient Safety Scientist to lead complex pharmacovigilance (PV) projects within the Oncology Patient Safety team, based in Barcelona, Spain.

The QARA Specialist will maintain and ensure the company's quality system complies with FDA, EU, ISO 13485, IEC 62304, and international medical device and IVD requirements.

AstraZeneca's CVRM Biometrics team is hiring a Statistical Programming Associate Director to lead and oversee statistical programming deliverables for clinical drug development programs.

TFS HealthScience is seeking a Site Coordinator to support clinical trial site activities in Madrid, Spain.

Biorce, a HealthTech company in Barcelona, is hiring a Clinical Specialist to support its Scientific function, reporting to the Chief Scientific Officer.